Image diagnoses for "Macule", "red"
187 results with 616 images

Ulerythema ophryogenes. extensive erythema with (scarred) raeration of the eyebrows. between the still persistent eyebrows are dense, fine, hairless follicular papules.

Vasculitis leukocytoclastic (non-IgA-associated): small spotted vasculitis of both lower legs; multiple red spots (redness cannot be suppressed).

AL-amyloidosis in smoldering myeloma. 77-year-old patient with recurrent ecchymosis of the periorbital region, clinically corresponding to a hematoma of the eyeglasses. These characteristic skin lesions are called "raccoon sign". Further purple skin lesions are found in the neck and retroauricularly. The bone marrow biopsy showed a smoldering myeloma (infiltration of plasma cells at 15%).

Teleangiectasia macularis eruptiva perstans: discrete, moderately itchy, disseminated, 0.2-0.5 cm large, roundish, red or reddish-brown spots interspersed with telangiectasia; urticarial reaction when rubbed vigorously over the spot (Darier's sign).

Dermatomyositis: Flat red plaques on the end phalanges. Hyperkeratotic nail folds

haematoma, nail haematoma. nail alteration after slight crush trauma. striped, red and blue-black spots (splinter hemorrhages). since red and black shades are present at the same time, this finding speaks against a melanotic pigmentation.

Dermatitis, phototoxic. pronounced erythema on the left forearm in a 71-year-old patient who had sunbathed while undergoing doxycycline therapy.

Teleangiectasia macularis eruptiva perstans. 58-year-old patient with a generalized, flekc-shaped clinical picture which has existed for years and shows a constant progression. itching during sweat-inducing efforts and mechanical exposure of the affected skin areas. close-up with bizarre teleangiectatic vessel convolutions.

Purpura thrombocytopenic: Hemorrhagic spots with a tendency to confluence, existing on both lower legs with emphasis on the extensor sides. It is a drug-induced form of a thrombotic- thrombocytopenic purpura with hemolytic microangiopathic anemia and central nervous failure symptoms. The trigger was the ingestion of non-steroidal anti-inflammatory drugs. Sudden onset with fever, disorientation, stupor.

Erythronychia, localized longitudinal detail magnified by reflected light microscopy; solitary, painless, red longitudinal striation of the nail plate with slight, V-shaped retraction and several splinter hemorrhages.

mononuleosis, infectious. generalized (almost universal) macular exanthema. raspberry tongue with swollen papillae. tongue surface completely free of coating.

Vasculitis leukocytoclastic (non-IgA-associated): multiple, for about 10 days existing, localized on both lower legs, irregularly distributed, 0.1-0.2 cm large, confluent in places, symptomless, red, smooth spots (not compressible).

Eczema atopic (erythrodermal): severe, universal (erythrodermal) atopic eczema, exacerbation phase for about 3 months.

Spider veins. Multiple, radially spread, radiating vascular dilatations of different calibre, partly in the skin level, without symptoms, persisting for several years, as if drawn with a thin pencil, located at the level of the skin, on the integument of a 77-year-old female patient. In the centre confluence of the filigree vascular strands to a bluish red spot.

Purpura Schönlein-Henoch. seeding of smallest petechiae beside fresh and older haemorrhagic maculae.

Tinea inguinalis: plaques that have existed for several months, coarse lamellar scaling and moderately itchy. Mycological evidence of T. rubrum.

Vasculitis, leukocytoclastic (non-IgA-associated). multiple, acute, symmetric, since 2 weeks existing, localized on both lower legs, irregularly distributed, 0.1-0.2 cm large, sharply defined, symptomless, hemorrhagic spots and blisters as well as beginning incrustations.

Dermatitis chronic actinic. detail enlargement: Disseminated, scratched papules and nodules as well as blurred, large-area, red, sharply itching fine-lamellar scaling spots and plaques in the face of a 51-year-old female patient with atopic eczema existing since birth.

Epidermolysis bullosa simpex, Weber-Cockayne: after banal traumas visible blistering or only simple detachment of the epidermis. scarless healing.